Mondial CRx
Who Is the Company Behind Mondial CRx?
- Seller: Mondial Software
- Year Founded: 2019
- HQ Location: Bedford, US
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LinkedIn® Page: www.linkedin.com
17 employees on LinkedIn®
Total Products under this Category: 182
Last updated: September 06, 2026
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Highlighted products: OnCore CTMS, Viedoc, Clinical Research Suite, Florence eBinders, Rave CTMS, Clario CTMS, Vial EDC + eSource, and TrialHub.
Underlying data: [Grid® JSON](https://www.g2.com/categories/clinical-trial-management-systems/grids.json?focus%5B%5D=oncore-ctms&focus%5B%5D=viedoc&focus%5B%5D=clinical-research-suite&focus%5B%5D=florence-healthcare-florence-ebinders&focus%5B%5D=rave-ctms&focus%5B%5D=clario-ctms&focus%5B%5D=vial-edc-esource&focus%5B%5D=trialhub)
Patient pre-screening AI assistant for clinical trial recruitment.
An innovative, no-code platform for conducting participant-centric digital clinical trials in record time. Collect eConsent, ePROs, and wearable device data from Fitbit, Garmin, Oura, Apple Watch, Google Fit and more. Connect to EHR and claims records for a more robust longitudinal record of each participant. All data is stored in the HIPAA-compliant, Meaningful Use Certified EDC HIEBus™ platform, and is then exported to researchers in an easy-to-use format, allowing scientists to focus on science.
oomnia is a real-time SaaS platform that unifies all essential clinical trial tools-EDC, RTSM, CTMS, eTMF, eCOA, ePRO, and eConsent-into one cohesive system. With single sign-on, users save up to 75% of time spent navigating between systems. Its multi-tenant design allows stakeholders to manage multiple trials on a single instance and gain oversight of entire portfolios. No coding is required due to intuitive drag-and-drop features. oomnia is fully interoperable, eliminating integration issues, and offers role-based access with a user-friendly interface customizable by language and notifications. Real-time reporting, seamless randomization, and complete audit logs enhance efficiency and data accuracy. The platform complies with 21 CFR Part 11, EU Annex 11, and CDISC standards. ISO 27001 and ISO 9001 certified and FDA/Swissmedic inspected, oomnia enables up to 50% time and cost savings through streamlined, intelligent trial management.
Centralized Monitoring Built for Modern Clinical Trials Improve trial performance by up to 30% with monitoring that reduces complexity and keeps your study on track. Focus on what matters most • Vizualize changes over time instantly • Quickly identify critical risks by uncovering hidden insights • Minimize wasted effort by directing attention where it’s needed Confidence in every decision • Full visibility with intelligent, dynamic data structures • Adapt easily to emerging needs and regulatory expectations • Demonstrate compliance with a clear evidence trail Efficiency across the board • Repetitive monitoring tasks are automated • Periodic review cycles are streamlined • Free up time and resources to concentrate on high-value activities